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Reference

Evidence

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Outcomes
Proteins
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Reactions
Reach

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Processes
Anatomy
Cell types
Organisms
Materials
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Diseases

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A reference for what the literature reports. Not medical advice.

Disease

narcolepsy 3

MONDO:0012179Mondo

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Findings

No curated finding names narcolepsy 3 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

A rare, autosomal dominant form of narcolepsy mapped to chromosome 21q, between genetic markers D21S267 and ABCG1. 6 patients with the milder form were DQB1*0602-positive.

Definition from the Mondo Disease Ontology (MONDO:0012179), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: hereditary narcolepsy
hereditary neurological disease
narcolepsy-cataplexy syndrome

Other names

1 name

Resolves to: narcolepsy 3

Also called: NRCLP3